MYSOLINE
Pronunciation: PRI-mi-doen


What it isDeoxybarbiturate antiepileptic that is active on its own; only 15–25% is oxidized to phenobarbital, most of a dose leaves unchanged, and the largest metabolite, PEMA, is inert in tremor.
Why this oneWith propranolol it is one of only two first-line treatments for essential tremor, and the tremor effect is primidone’s own: one dose quiets tremor for up to a day while phenobarbital and PEMA are still barely measurable. Not a controlled substance.
What limits itA severe acute reaction on the first dose is common, so start at a fraction of the target. It is an enzyme inducer through its phenobarbital metabolite.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Epilepsy (grand mal, psychomotor, focal), no prior treatment | Adult & child ≥8 yr | 100-125 mg QHS | 250 mg TID | 500 mg QID (2000 mg/day) |
| Epilepsy | Pediatric <8 yr | 50 mg QHS | 125-250 mg TID (or 10-25 mg/kg/day divided) | 250 mg TID |
Titration Increase approximately every 3 days per initiation schedule (Days 1-3, 4-6, 7-9, then maintenance)
Renal Undefined
Hepatic Undefined
Target serum primidone level 5-12 mcg/mL
Available strengths
Pregnancy Undefined
Lactation Undefined
Generic entry2001
NO BOXED WARNINGS
Principal riskSedation; converts to phenobarbital
Legacy pregnancy categoryD
Defining liabilitySedation, dependence and phenobarbital-mediated respiratory/CNS depression in overdose.
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